Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Merge OrthoPACS software. The firm name on the label is Merge Healthcare Recalled by Merge Healthcare, Inc. Due to Studies that have QC, PDE, or HL7 ADT...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Merge Healthcare, Inc. directly.
Affected Products
Merge OrthoPACS software. The firm name on the label is Merge Healthcare, Hartland, WI.
Quantity: 160 sites potentially have the affected versions
Why Was This Recalled?
Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate via telmed protocol to the destination server and may fail to import on the destination server.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Merge Healthcare, Inc.
Merge Healthcare, Inc. has 93 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report